{
    "disease_id": "DOID:1206",
    "recommended_name": {
        "id": "DOID:1206",
        "resource": "Disease Ontology",
        "url": "http://disease-ontology.org/term/DOID:1206",
        "name": "Rett syndrome",
        "description": "A pervasive developmental disease that is characterized by normal early growth and development followed by a slowing of development, loss of purposeful use of the hands, distinctive hand movements, slowed brain and head growth, problems with walking, seizures, and intellectual disability."
    },
    "synonyms": [
        {
            "id": "DOID:1206",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1206",
            "name": "Rett's disorder",
            "description": ""
        },
        {
            "id": "DOID:1206",
            "resource": "Disease Ontology",
            "url": "http://disease-ontology.org/term/DOID:1206",
            "name": "cerebroatrophic hyperammonemia",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "Rett syndrome",
            "description": "A severe neurodevelopmental disorder affecting the central nervous system."
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "Rett syndrome",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "Rett's disorder",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "cerebroatrophic hyperammonemia",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "rett syndrome, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "rett syndrome, atypical, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "rett syndrome, preserved speech variant, X-linked dominant",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "RTT",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "Rett syndrome, Zappella variant",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "Rett syndrome, atypical",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "Rett syndrome, preserved speech variant",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "Rts",
            "description": ""
        },
        {
            "id": "MONDO:0010726",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0010726",
            "name": "autism, dementia, ataxia, and loss of purposeful hand use",
            "description": ""
        },
        {
            "id": "MONDO:0013270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013270",
            "name": "Rett syndrome, congenital variant",
            "description": ""
        },
        {
            "id": "MONDO:0013270",
            "resource": "MONDO",
            "url": "https://monarchinitiative.org/disease/MONDO:0013270",
            "name": "Rett syndrome, congenital variant",
            "description": ""
        },
        {
            "id": "MIM:312750",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/312750",
            "name": "Rett syndrome",
            "description": "Rett syndrome"
        },
        {
            "id": "MIM:613454",
            "resource": "MIM",
            "url": "https://www.omim.org/entry/613454",
            "name": "Rett syndrome congenital variant",
            "description": "Rett syndrome congenital variant"
        }
    ]
}